Both Stat5a and Stat5b are required for antigen-induced eosinophil and T-cell recruitment into the tissue

As the magnitude of antigen-induced eosinophil recruitment into the airways differs depending on a genetic background of mice (our unpublished data), Stat5a-deficient mice (Stat5a^−/−, ref. 21) and Stat5b-deficient mice (Stat5b^−/−, ref. 22) were back-crossed to BALB/c mice (Charles River Laboratories, Atsugi, Japan) for 4 generations. All mice were H-2^d/d and littermate wild-type mice were used as a control. In preliminary experiments, we found that the littermate control wild-type mice exhibited indistinguishable responses to those seen with BALB/c mice in our assays; antigen-induced eosinophil and T-cell recruitment into the airways, titer of antigen-specific IgE antibody, and in vitro cytokine production and proliferation of splenocytes (data not shown). Mice were housed in microisolator cages under pathogen-free conditions. All experiments were performed according to the guidelines of Chiba University. The mice were genotyped by PCR of tail DNA, using the following primer pairs: To detect Stat5a wild-type gene, 5′-CTTTATTGATAACGATCTATCCCTCACCC-3′ and 5′-CTCCACTCTGCAGAGTCTATGGAATCC-3′; to detect Stat5a-deficient gene, 5′-GCTGACAGCCGGAACACGGCGG-3′ and 5′-GTGCAATCCATCTTGTTCAATGGCCG-3′; to detect Stat5b wild-type gene, 5′-CAGGAGGGATCCAGTGCCAGC-3′ and 5′-TGGCTCTACAGTGAGTTTGGT-3′; to detect Stat5b-deficient gene, 5′-GACTTGGAGATTGCCAACCCATATCTAAGT-3′ and 5′-TGAGCCGAAGGTGTAGTCGGAGTTTGCATT 3′.

Mice (age 7-8 weeks) were immunized intraperitoneally twice with 4 μg of ovalbumin (OVA) (Sigma Chemical Co, St. Louis, MO) in 4 mg of aluminum hydroxide at a 2-week interval. Twelve to 14 days after the second immunization, the sensitized mice were challenged with aerosolized OVA as described below.

The eosinophil infiltration into the airways was induced by the inhalation of antigen in sensitized mice, and the number of eosinophils infiltrating into the submucosal tissue of trachea was evaluated as described previously.6 Briefly, the sensitized mice were given aerosolized OVA (50 mg/mL) dissolved in 0.9% saline by a DeVilbiss 646 nebulizer (DeVilbiss Corp, Somerset, PA) for 20 minutes. As a control, 0.9% saline alone was administered by the nebulizer. At 24 or 48 h after the inhalation, the tracheas were excised, fixed in 10% buffered-formalin, and embedded in paraffin. The specimens (3 μm thick) were stained with Luna solution and hematoxylin-eosin solution. The number of eosinophils in the submucosal tissue of trachea was counted in Luna-stained sections and expressed as the number of eosinophils per the length of the basement membrane of trachea, which was measured with a digital curvimeter.

The eosinophil and T-cell infiltration into the bronchoalveolar lavage fluid (BALF) was also evaluated as described previously.28In short, bronchoalveolar lavage was performed with 1.2 mL of phosphate-buffered saline (PBS) at 24 or 36 hours after saline or OVA inhalation. BALF was centrifuged at 400g for 5 minutes at 4°C, and cell differentials were determined by counting 500 cells stained with Wright-Giemsa solution. A fraction of the cells were subjected to a flow cytometric analysis for the lymphocyte surface phenotyping of CD4 and CD8, as described below.

The BALF was centrifuged at 400g for 5 minutes at 4°C, and the amount of IL-5 in the supernatant was measured by the enzyme immunoassay, according to the manufacturer's instruction (PharMingen, San Diego, CA). The assays were performed in duplicate.

The spleen was removed from OVA-sensitized mice and a single cell suspension of splenocytes was prepared. Splenocytes (2 × 10⁵) were then suspended in 200 μL of RPMI 1640 medium supplemented with 10% FCS (GIBCO BRL, Rockville, MD), 10 mmol/L glutamine, 100 U/mL penicillin, and 100 μg/mL streptomycin and were cultured in triplicate in the absence or presence of OVA (200 μg/mL) in a 96-well microtiter plate for 72 hours. In some experiments, splenocytes (2 × 10⁵) were also cultured for 72 hours in a 96-well microtiter plate coated with 5 μg/mL of anti-CD3ε mAb (145-2C11, PharMingen). The culture supernatant was collected and the amounts of IL-4, IL-5, and IFN-γ were determined by enzyme-linked immunosorbent assay (ELISA) according to the manufacturer's instructions (PharMingen). For proliferation assays, splenocytes (2 × 10⁵) were cultured in the same conditions as described previously, with 1 μCi (0.037 MBq)³H] thymidine added for the final 16 hours.

Two weeks after the second immunization, the titer of OVA-specific IgE antibody in mouse serum was assessed by a 24-hour passive cutaneous anaphylaxis (PCA) reaction as described by Ovary.29 

The amount of OVA-specific IgG1 and IgG2a in serum was measured by ELISA as described elsewhere.30 In brief, ELISA plates were coated with OVA (250 μg/mL), washed 3 times with PBS containing 0.05% Tween20 (PBST), and blocked with blocking buffer (PBS containing 2% bovine serum albumin [BSA; Sigma Chemical Co]). Serum samples were added to the wells after 1:1000 or 1:3000 dilution in blocking buffer. As a control, serial dilution of pooled serum from OVA-sensitized wild-type mice were analyzed in each plate. After 1-hour incubation, wells were washed with PBST, added either biotinylated antimouse IgG1 (PharMingen) or biotinylated antimouse IgG2a (PharMingen) at 2 μg/mL in blocking buffer, and incubated for 1 hour. After washing, wells were incubated with 100 μL of ExtrAvidin alkaline phosphatase (1:2000 dilution, Sigma Chemical Co, St Louis, MO) for 45 minutes, washing with PBST, and the reaction was developed with pNPP (Sigma Chemical Co).

IL-5–induced eosinophilopoiesis was analyzed as described previously.26 In brief, mice were injected intraperitoneally with 20 000 U of recombinant murine IL-5 (rmIL-5)26 daily for 4 days. Forty-eight hours after the fourth administration of rmIL-5, mice were killed and cell differentials in bone marrow, peripheral blood, and peritoneal cavity were determined by counting 500 cells stained with Wright-Giemsa solution. A part of the cells in the peritoneal cavity were subjected to a flow cytometric analysis for the surface phenotyping of VLA-4 and Gr-1 as described below.

Cells from the BALF and peritoneal cavity were stained and analyzed on a FACScaliber (Becton Dickinson, San Jose, CA) with CELLQuest software.24 For direct staining, the following conjugated antibodies were purchased from PharMingen: anti-CD4 FITC (H129.19), anti-CD8 APC, 53-6.7 anti-VLA-4 FITC (R1-2), and anti-Gr-1 APC (RB6-8C5). Before staining, Fc receptors were blocked with anti-CD16/32 antibody (2.4G2, PharMingen).

Data are summarized as mean ± SD. The statistical analysis of the results was performed by the unpaired t test. Pvalues < .05 were considered significant.

Because Stat5 is activated in response to IL-520 and IL-5 is known to be vital for antigen-induced eosinophil recruitment into the airways,6 we first determined whether antigen-induced eosinophil recruitment into the airways was normal in Stat5a-deficient (Stat5a^−/−) mice and in Stat5b-deficient (Stat5b^−/−) mice. As shown in Figure 1A, antigen-induced eosinophil infiltration into the trachea at 24 hours after antigen inhalation was severely diminished in both Stat5a^−/− mice and Stat5b^−/− mice by 85% and 84%, respectively (wild-type mice 17.2 ± 5.2, Stat5a^−/−mice 2.5 ± 1.4, and Stat5b^−/− mice 2.8 ± 1.0 eosinophils/mm, mean ± SD, n = 8 mice in each group, P < .001). Antigen-induced eosinophil infiltration into the trachea at 48 hours was also significantly diminished in Stat5a^−/− mice and Stat5b^−/− mice (data not shown). Consistent with diminished antigen-induced eosinophil infiltration in the trachea, the number of eosinophils recovered in BALF at 36 hours after antigen inhalation was also significantly decreased in Stat5a^−/− mice and Stat5b^−/− mice by 70% and 74%, respectively (n = 5, P < .005) (Figure 1B).

FACS analysis of BALF cells revealed that antigen-induced CD4⁺ T-cell infiltration into the airways at 24 hours was also decreased in both Stat5a^−/− mice and Stat5b^−/− mice by 64% and 61%, respectively (n = 5, P < .005) (Figure 2). In addition, consistent with diminished CD4⁺ T-cell infiltration in the airways, IL-5 levels in the BALF at 24 hours after antigen challenge were decreased in Stat5a^−/−mice and Stat5b^−/− mice by 57% and 59%, respectively (wild-type mice 549 ± 98, Stat5a^−/− mice 239 ± 90, and Stat5b^−/− mice 227 ± 86 pg/mL, n = 5,P < .005) (Figure 3). Taken together, these results suggest that both Stat5a and Stat5b are required for antigen-induced eosinophil and T-cell recruitment into the airways and that diminished antigen-induced eosinophil recruitment in Stat5a^−/− mice and Stat5b^−/− mice results in part from impaired IL-5 production in the airways.

We then examined the Th1 cell and Th2 cell development in Stat5a^−/− mice and Stat5b^−/− mice. As shown in Table1, IL-4 and IL-5 production from antigen (OVA)-stimulated splenocytes was undetectable in Stat5a^−/− mice and Stat5b^−/− mice, whereas antigen-stimulated wild-type splenocytes produced substantial amounts of IL-4 and IL-5 (n = 5, P < .01). Similarly, IFN-γ production from antigen-stimulated splenocytes was undetectable in Stat5a^−/− mice and Stat5b^−/− mice but was readily detected in antigen-stimulated wild-type splenocytes (n = 5, P < .01) (Table 1).

Although similar numbers of T cells were found in splenocytes from wild-type mice, Stat5a^−/− mice, and Stat5b^−/− mice (data not shown), it was possible that antigen-specific T cells were decreased in Stat5a^−/− mice and Stat5b^−/− mice. To determine whether the defects in cytokine production from antigen-stimulated splenocytes in Stat5a^−/− mice and Stat5b^−/− mice resulted from the impaired generation of an antigen-specific T-cell pool, we analyzed cytokine production from anti-CD3–stimulated splenocytes. IL-4 production from anti-CD3–stimulated splenocytes was approximately 90% reduced in both Stat5a^−/− mice and Stat5b^−/− mice, compared with IL-4 production in wild-type mice (n = 5, P < .001) (Table 1). IL-5 production from anti-CD3–stimulated splenocytes was also similarly decreased in Stat5a^−/− mice and Stat5b^−/− mice by approximately 80% (n = 5,P < .001) (Table 1). In contrast, IFN-γ production from anti-CD3–stimulated splenocytes was normal in Stat5a^−/− mice and but moderately diminished in Stat5b^−/− mice by 41% (n = 5,P < .01) (Table 1).

Given the importance of IL-2 in T-cell proliferation31and the ability of IL-2 to potently activate Stat5a and Stat5b,32-34 we next examined whether antigen-induced proliferation of splenocytes was normal in these mice. Antigen-induced proliferation of splenocytes was substantially observed in wild-type mice, whereas antigen-induced proliferation of splenocytes was significantly decreased in Stat5a^−/− mice and Stat5b^−/− mice by 79% and 81%, respectively (n = 5, P < .005) (Figure4A). This defect may account for the diminished antigen-induced T-cell infiltration into the airways (Figure2). In contrast to the diminished antigen-induced proliferation, anti-CD3–induced proliferation of splenocytes was normal in Stat5a^−/− mice and slightly decreased (but not statistically significant) in Stat5b^−/− mice (n = 5) (Figure 4B). These results suggest that Stat5a and Stat5b might be required for the generation of antigen-specific T-cell pools in the periphery.

It has been shown that antigen-specific IgE production is a marker of systemic Th2 responses,35 but it is not essential for antigen-induced airway eosinophilia in mice36,37 (and our unpublished data). Therefore, we examined antigen-specific IgE production in Stat5a^−/− mice and Stat5b^−/− mice at 2 weeks after the second immunization. Interestingly, Stat5a^−/− mice exhibited decreased levels of antigen-specific IgE production (n = 10, P < .005), whereas antigen-specific IgE production was normal in Stat5b^−/− mice (Figure5A). In addition, antigen-specific IgG1 production was also diminished in Stat5a^−/−mice (n = 10, P < .01) (Figure 5B), suggesting that systemic Th2 response was diminished in Stat5a^−/− mice but not in Stat5b^−/− mice. In contrast to the diminished IgE and IgG1 production in Stat5a^−/− mice, antigen-specific IgG2a production was increased in Stat5a^−/− mice (n = 10, P < .005) (Figure 5C), suggesting the Th1-polarized immune responses in Stat5a^−/− mice.

Although the diminished antigen-induced eosinophil recruitment into the airways in Stat5a^−/− mice and Stat5b^−/− mice (Figure 1) presumably results in part from diminished IL-5 production in the airways (Figure 3), the defect in eosinophil recruitment into the airways appeared more severe than the defect in IL-5 production. We therefore investigated whether IL-5-dependent eosinophilopoiesis was normal in Stat5a^−/− mice and Stat5b^−/− mice. To address this issue, Stat5a^−/− mice and Stat5b^−/− mice were injected intraperitoneally with recombinant murine IL-5 (rmIL-5; 20 000 U/d) for 4 days and the eosinophil numbers in the bone marrow, peripheral blood, and peritoneal cavity were determined at 48 hours after the last injection. The administration of rmIL-5 significantly increased eosinophil numbers in the bone marrow in wild-type mice (n = 5) (Figure6A). In Stat5a^−/−mice and Stat5b^−/− mice; however, the magnitude of the IL-5-induced eosinophilia in the bone marrow was approximately half of that in rmIL-5–treated wild-type mice (n = 5,P < .005) (Figure 6A). These results indicate that both Stat5a and Stat5b play a role in IL-5-dependent eosinophilopoiesis.

The eosinophil numbers in the peripheral blood and the peritoneal cavity were also significantly increased by the intraperitoneal injection of rmIL-5 in wild-type mice (Figure 6B and C). Although eosinophil numbers in the peripheral blood were similarly increased by the administration of rmIL-5 among the 3 groups of mice (Figure 6B), however, the eosinophil numbers in the peritoneal cavity were significantly decreased in Stat5a^−/− mice and Stat5b^−/− mice by 59% and 57%, respectively (n = 5, P < .005) (Figure 6C). Consistent with increased eosinophils in the peritoneal cavity in rmIL-5–treated wild-type mice, FACS analysis revealed that the Gr-1^mid VLA-4⁺population (R1 region), which most likely represents eosinophils,38 was selectively increased in the peritoneal cavity after rmIL-5 administration (Figure7). In contrast, the Gr-1^highVLA-4⁻ population (R2 region), which most likely represents neutrophils,38 was not increased in the peritoneal cavity on rmIL-5 administration (Figure 7). Consistent with the diminished eosinophils in the peritoneal cavity of rmIL-5–treated Stat5a^−/− mice or Stat5b^−/− mice, the fraction of Gr-1^mid VLA-4⁺ cells in the peritoneal cavity was also diminished in Stat5a^−/− and Stat5b^−/− mice (Figure 7). These results suggest that, in addition to the role in IL-5–induced eosinophilopoiesis, Stat5a and Stat5b may be necessary for IL-5–induced chemotaxis of eosinophils.

It has been shown that antigen-induced eosinophil recruitment into the airways of sensitized mice is mediated by the Th2 subset of CD4⁺ T cells and subsequent secretion of IL-5.6 In this study, we showed that both Stat5a and Stat5b were required for antigen-induced eosinophil and T-cell recruitment into the airways. We found that antigen-induced eosinophil infiltration in the airways and antigen-induced CD4⁺ T-cell infiltration and IL-5 production in the airways were diminished in both Stat5a^−/− mice and Stat5b^−/− mice. Moreover, we found that antigen-induced proliferation of splenocytes was diminished in Stat5a^−/− mice and Stat5b^−/− mice, suggesting that the generation of antigen-primed T cells might be compromised in Stat5a^−/− mice and Stat5b^−/− mice. This defect may be due to diminished IL-2–induced proliferation of T cells in Stat5a^−/− mice24 and Stat5b^−/− mice23 and may account for the diminished antigen-induced T-cell infiltration into the airways. Finally, we found that IL-5–dependent eosinophilopoiesis was impaired in Stat5a^−/− mice and Stat5b^−/− mice. Therefore, these results indicate that the diminished antigen-induced eosinophil recruitment into the airways in Stat5a^−/− mice and Stat5b^−/− mice results from both impaired IL-5 production in the airways and impaired IL-5 responsiveness of eosinophils.

Given that Stat5a and Stat5b are highly homologous and exhibit overlapping functions,18,25 it was surprising that antigen-induced eosinophil and T-cell recruitment into the airways was severely impaired in mice lacking either Stat5a or Stat5b. Because Stat5b DNA binding activity is not dependent on the presence of Stat5a,24 it is possible that the residual eosinophil recruitment in Stat5a^−/− mice is regulated by intact Stat5b. However, it is also possible that the residual eosinophil recruitment in Stat5a^−/− mice or Stat5b^−/− mice is regulated by Stat5-independent signaling pathway(s). This can be further assessed when Stat5a/Stat5b double-deficient mice in the BALB/c background are available. Nevertheless, it may be predicted that antigen-induced eosinophil recruitment into the airways, which is regulated by CD4⁺ T cells,6 is greatly diminished in Stat5a/Stat5b double-deficient mice, because TCR-mediated proliferation of CD4⁺ T cells from Stat5a/Stat5b double-deficient mice is defective.25 

We also found that IL-5-induced in vivo eosinophilopoiesis was diminished in Stat5a^−/− mice and Stat5b^−/− mice. IL-5 acts on eosinophil precursors, resulting in induction of proliferation and differentiation into mature eosinophils.39 It has been reported that bone marrow cells from IL-5Rα^−/−mice26 or IL-5^−/−mice7,27 fail to form eosinophilic colonies in response to IL-5 or parasite infection. GM-CSF also plays an important role in the production of eosinophils in bone marrow.40IL-5, GM-CSF, and IL-3 all share common β chain (βc) as a receptor component41 and activate Jak2 and Stat5a/Stat5b.16-18,20 Recently, Feldman et al42 demonstrated that GM-CSF-induced proliferation of bone marrow-derived macrophages is diminished in Stat5a^−/− mice, suggesting that Stat5a plays a role in βc-dependent proliferation. In contrast, it has been reported that in vitro IL-5–induced colony formation from bone marrow cells is normal in Stat5a^−/− mice and Stat5b^−/− mice.43 At present, the precise mechanism(s) underlying the discrepancy between the in vivo and the in vitro requirement for Stat5a/Stat5b in IL-5–induced eosinophilopoiesis is unclear. However, it is likely that the compensatory role of Stat5a by Stat5b or Stat5b by Stat5a is not sufficient for in vivo IL-5–induced eosinophilopoiesis, because IL-5–dependent in vitro colony formation is diminished in Stat5a/Stat5b double-deficient mice.43 In addition, our finding of diminished eosinophil numbers in the peritoneal cavity after IL-5 administration in Stat5a^−/− mice and Stat5b^−/− mice suggest that Stat5a and Stat5b may also be necessary for IL-5–induced chemotaxis of eosinophils.44 

Interestingly, we found that IL-4 production from anti-CD3–stimulated splenocytes was diminished in Stat5a^−/− mice. We also found that antigen-specific IgE and IgG1 production was diminished in Stat5a^−/− mice, whereas antigen-specific IgG2a production was increased in Stat5a^−/− mice. Therefore, in Stat5a^−/− mice, the balance between Th1 and Th2 cell activation is biased toward a Th1 profile, suggesting that Stat5a may be involved in the IL-4–dependent Th2 cell development. Consistent with this finding, it has recently been shown that IL-4 signaling activates Stat5 as well as Stat6.45 In contrast, in Stat5b^−/− mice, the situation may be more complicated. In these mice, although anti-CD3–induced IL-4 production from splenocytes was diminished, antigen-specific IgE production in vivo was normal. Because anti-CD3–induced IFN-γ production was also slightly diminished in Stat5b^−/− mice, it is possible that the balance between IL-4 and IFN-γ rather than the amount of IL-4 may be critical for in vivo IgE production. Alternatively, it is conceivable that the discrepancy may result from compensatory role(s) of other cytokines such as IL-13.46 

As discussed previously, diminished antigen-induced eosinophil recruitment into the airways is likely to result from both impaired IL-5 production by T cells and impaired IL-5 responsiveness of eosinophils in Stat5a^−/− mice and Stat5b^−/− mice. However, other cell populations may also be involved in the diminished antigen-induced eosinophil recruitment into the airways. Recently, it has been shown that γδ T cells47 and NK cells48,49 play important role(s) in allergic inflammation. Because γδ T cells are diminished in Stat5a^−/− mice24 and NK cell function is particularly impaired in Stat5b^−/−mice,23 these defects may be responsible for the diminished antigen-induced eosinophil recruitment into the airways.

In this study, we provide the evidence that Stat5a and Stat5b are important for allergic inflammation. Recently, several lines of evidence have indicated that other STAT proteins besides Stat5 also play important immunopathogenic roles in the development of allergic inflammation. Stat6 has been shown to play an important role in causing allergic inflammation,50,51 probably by generating antigen-specific Th2 cells.52-54 These observations may be consistent with the finding that IL-13, which activates Stat6,46 plays a role in allergic inflammation.55,56 In contrast, because Stat4 is activated by IL-12 and is essential for Th1 cell differentiation57,58and because IL-12 is shown to exhibit inhibitory effects on allergic inflammation,28,59 Stat4 may play a role in prevention of allergic inflammation. More recently, Sampath et al60demonstrated that Stat1 was activated in epithelial cells in patients with asthma, correlating with ICAM-1 expression and T-cell infiltration. Although the target genes of these STAT proteins for allergic inflammation remain unclear, more detailed mechanism(s) may be revealed using these mutant mice.

In conclusion, from the analysis of Stat5a^−/−mice and Stat5b^−/− mice, we have established several important points. First, both Stat5a and Stat5b are vital for antigen-induced T-cell infiltration and IL-5 production in the airways and thereby play an important role in causing antigen-induced eosinophil recruitment into the airways. Second, our data provide in vivo evidence that both Stat5a and Stat5b are required for IL-5–induced eosinophilopoiesis. Third, although the precise mechanism(s) is at present unclear, Stat5a is important for the determination of Th1/Th2 balance on antigen sensitization. Finally, our results suggest that specific inactivation of Stat5 proteins in the tissue could potentially represent a basis for the treatment of allergic inflammation.

We thank Drs L. Hennighausen and X. Liu for Stat5a-deficient mice and K. Kurasawa, M. Nishimura, T. Sato, K. Hirano, T. Matsui, and M. Watanabe for technical help.